PubMed

Recessive Mutations of the Gene TRPM1 Abrogate ON Bipolar Cell Function and Cause Complete Congenital Stationary Night Blindness in Humans.

Li Z, Sergouniotis PI, Michaelides M, Mackay DS, Wright GA, Devery S, Moore AT, Holder GE, Robson AG, Webster AR.

Am J Hum Genet. 2009 Nov;85(5):711-9. Epub 2009 Oct 29.PMID: 19878917 [PubMed - in process]Related articles

An unusual fundus phenotype of inner retinal sheen in X-linked retinoschisis.

Robson AG, Mengher LS, Tan MH, Moore AT.

Eye (Lond). 2009 Sep;23(9):1876-8. Epub 2008 Dec 5. No abstract available. PMID: 19741719 [PubMed - in process]Related articles

Clinicopathological case series of four patients with inherited macular disease.

Wickham L, Chen FK, Lewis GP, Uppal GS, Neveu MM, Wright GA, Robson AG, Webster AR, Grierson I, Hiscott P, Coffey PJ, Holder GE, Fisher SK, Da Cruz L.

Invest Ophthalmol Vis Sci. 2009 Aug;50(8):3553-61. Epub 2009 Mar 11.PMID: 19279306 [PubMed - indexed for MEDLINE]Related articles

Electrodiagnostic assessment in optic nerve disease.

Holder GE, Gale RP, Acheson JF, Robson AG.

Curr Opin Neurol. 2009 Feb;22(1):3-10. Review.PMID: 19155758 [PubMed - indexed for MEDLINE]Related articles

Effects of cystic fibrosis lung disease on gas mixing indices derived from alveolar slope analysis.

Horsley AR, Macleod KA, Robson AG, Lenney J, Bell NJ, Cunningham S, Greening AP, Gustafsson PM, Innes JA.

Respir Physiol Neurobiol. 2008 Aug 31;162(3):197-203. Epub 2008 Jun 25.PMID: 18625345 [PubMed - indexed for MEDLINE]Related articles

Measurement of macular pigment optical density and distribution using the steady-state visual evoked potential.

Robson AG, Parry NR.

Vis Neurosci. 2008 Jul-Aug;25(4):575-83. Epub 2008 Jul 11.PMID: 18620612 [PubMed - indexed for MEDLINE]Related articles

Using laboratory measurements to predict in-flight desaturation in respiratory patients: are current guidelines appropriate?

Robson AG, Lenney J, Innes JA.

Respir Med. 2008 Nov;102(11):1592-7. Epub 2008 Jul 9.PMID: 18617380 [PubMed - indexed for MEDLINE]Related articles

ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicing.

Burgess R, MacLaren RE, Davidson AE, Urquhart JE, Holder GE, Robson AG, Moore AT, Keefe RO, Black GC, Manson FD.

J Med Genet. 2009 Sep;46(9):620-5. Epub 2008 Jul 8.PMID: 18611979 [PubMed - in process]Related articles

Phenotypic variation in enhanced S-cone syndrome.

Audo I, Michaelides M, Robson AG, Hawlina M, Vaclavik V, Sandbach JM, Neveu MM, Hogg CR, Hunt DM, Moore AT, Bird AC, Webster AR, Holder GE.

Invest Ophthalmol Vis Sci. 2008 May;49(5):2082-93.PMID: 18436841 [PubMed - indexed for MEDLINE]Related articlesFree article

Electrophysiological monitoring in a patient with an optic nerve glioma.

Moradi P, Robson AG, Rose GE, Holder GE.

Doc Ophthalmol. 2008 Sep;117(2):171-4. Epub 2008 Feb 27.PMID: 18301934 [PubMed - indexed for MEDLINE]Related articles

A new phenotype of macular dystrophy associated with a mitochondrial A3243G mutation.

Sivaprasad S, Kung BT, Robson AG, Black G, Webster AR, Bird A, Egan C.

Clin Experiment Ophthalmol. 2008 Jan-Feb;36(1):92-3. No abstract available. PMID: 18290960 [PubMed - indexed for MEDLINE]Related articles

Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways.

Bakrania P, Efthymiou M, Klein JC, Salt A, Bunyan DJ, Wyatt A, Ponting CP, Martin A, Williams S, Lindley V, Gilmore J, Restori M, Robson AG, Neveu MM, Holder GE, Collin JR, Robinson DO, Farndon P, Johansen-Berg H, Gerrelli D, Ragge NK.

Am J Hum Genet. 2008 Feb;82(2):304-19. Epub 2008 Jan 31.PMID: 18252212 [PubMed - indexed for MEDLINE]Related articlesFree article

Bilateral giant macular schisis in a patient with enhanced S-cone syndrome from a family showing pseudo-dominant inheritance.

Vaclavik V, Chakarova C, Bhattacharya SS, Robson AG, Holder GE, Bird AC, Webster AR.

Br J Ophthalmol. 2008 Feb;92(2):299-300. No abstract available. PMID: 18227217 [PubMed - indexed for MEDLINE]Related articles

The negative ERG: clinical phenotypes and disease mechanisms of inner retinal dysfunction.

Audo I, Robson AG, Holder GE, Moore AT.

Surv Ophthalmol. 2008 Jan-Feb;53(1):16-40. Review.PMID: 18191655 [PubMed - indexed for MEDLINE]Related articles

Biallelic mutation of BEST1 causes a distinct retinopathy in humans.

Burgess R, Millar ID, Leroy BP, Urquhart JE, Fearon IM, De Baere E, Brown PD, Robson AG, Wright GA, Kestelyn P, Holder GE, Webster AR, Manson FD, Black GC.

Am J Hum Genet. 2008 Jan;82(1):19-31.PMID: 18179881 [PubMed - indexed for MEDLINE]Related articlesFree article

Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update.

Robson AG, Michaelides M, Saihan Z, Bird AC, Webster AR, Moore AT, Fitzke FW, Holder GE.

Doc Ophthalmol. 2008 Mar;116(2):79-89. Epub 2007 Nov 6. Review.PMID: 17985165 [PubMed - indexed for MEDLINE]Related articlesFree article

Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophy.

Robson AG, Michaelides M, Luong VA, Holder GE, Bird AC, Webster AR, Moore AT, Fitzke FW.

Br J Ophthalmol. 2008 Jan;92(1):95-102. Epub 2007 Oct 25.PMID: 17962389 [PubMed - indexed for MEDLINE]Related articles

Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?

Audo I, Vanakker OM, Smith A, Leroy BP, Robson AG, Jenkins SA, Coucke PJ, Bird AC, De Paepe A, Holder GE, Webster AR.

Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4250-6.PMID: 17724214 [PubMed - indexed for MEDLINE]Related articlesFree article

Autofluorescence findings in acute exudative polymorphous vitelliform maculopathy.

Vaclavik V, Ooi KG, Bird AC, Robson AG, Holder GE, Webster AR.

Arch Ophthalmol. 2007 Feb;125(2):274-7. No abstract available. PMID: 17296907 [PubMed - indexed for MEDLINE]Related articles

Novel phenotypic and genotypic findings in X-linked retinoschisis.

Tsang SH, Vaclavik V, Bird AC, Robson AG, Holder GE.

Arch Ophthalmol. 2007 Feb;125(2):259-67.PMID: 17296904 [PubMed - indexed for MEDLINE]Related articlesFree article

Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutation.

Scott A, Strouthidis NG, Robson AG, Forsyth J, Maher ER, Schlottmann PG, Michaelides M.

Am J Ophthalmol. 2007 Feb;143(2):346-8. Epub 2006 Oct 23.PMID: 17258529 [PubMed - indexed for MEDLINE]Related articles

Assessment of patients with suspected non-organic visual loss using pattern appearance visual evoked potentials.

McBain VA, Robson AG, Hogg CR, Holder GE.

Graefes Arch Clin Exp Ophthalmol. 2007 Apr;245(4):502-10. Epub 2006 Nov 17.PMID: 17111152 [PubMed - indexed for MEDLINE]Related articles

Xanthophyll accumulation in the human retina during supplementation with lutein or zeaxanthin - the LUXEA (LUtein Xanthophyll Eye Accumulation) study.

Schalch W, Cohn W, Barker FM, Köpcke W, Mellerio J, Bird AC, Robson AG, Fitzke FF, van Kuijk FJ.

Arch Biochem Biophys. 2007 Feb 15;458(2):128-35. Epub 2006 Nov 7.PMID: 17084803 [PubMed - indexed for MEDLINE]Related articles

Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans.

Wu H, Cowing JA, Michaelides M, Wilkie SE, Jeffery G, Jenkins SA, Mester V, Bird AC, Robson AG, Holder GE, Moore AT, Hunt DM, Webster AR.

Am J Hum Genet. 2006 Sep;79(3):574-9. Epub 2006 Jul 24.PMID: 16909397 [PubMed - indexed for MEDLINE]Related articlesFree article

Chromatic VEP assessment of human macular pigment: comparison with minimum motion and minimum flicker profiles.

Robson AG, Holder GE, Moreland JD, Kulikowski JJ.

Vis Neurosci. 2006 Mar-Apr;23(2):275-83.PMID: 16638178 [PubMed - indexed for MEDLINE]Related articles

Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.

Robson AG, Saihan Z, Jenkins SA, Fitzke FW, Bird AC, Webster AR, Holder GE.

Br J Ophthalmol. 2006 Apr;90(4):472-9.PMID: 16547330 [PubMed - indexed for MEDLINE]Related articlesFree article

Unilateral electronegative ERG of non-vascular aetiology.

Robson AG, Richardson EC, Koh AH, Pavesio CE, Hykin PG, Calcagni A, Graham EM, Holder GE.

Br J Ophthalmol. 2005 Dec;89(12):1620-6.PMID: 16299143 [PubMed - indexed for MEDLINE]Related articlesFree article

Comparison of fundus autofluorescence and minimum-motion measurements of macular pigment distribution profiles derived from identical retinal areas.

Robson AG, Harding G, van Kuijk FJ, Pauleikhoff D, Holder GE, Bird AC, Fitzke FW, Moreland JD.

Perception. 2005;34(8):1029-34.PMID: 16178159 [PubMed - indexed for MEDLINE]Related articles

Electrophysiological characterisation and monitoring in the management of birdshot chorioretinopathy.

Holder GE, Robson AG, Pavesio C, Graham EM.

Br J Ophthalmol. 2005 Jun;89(6):709-18.PMID: 15923507 [PubMed - indexed for MEDLINE]Related articlesFree article

Retinal dysfunction and refractive errors: an electrophysiological study of children.

Flitcroft DI, Adams GG, Robson AG, Holder GE.

Br J Ophthalmol. 2005 Apr;89(4):484-8.PMID: 15774929 [PubMed - indexed for MEDLINE]Related articlesFree article

Comparison of fundus autofluorescence with photopic and scotopic fine-matrix mapping in patients with retinitis pigmentosa and normal visual acuity.

Robson AG, Egan CA, Luong VA, Bird AC, Holder GE, Fitzke FW.

Invest Ophthalmol Vis Sci. 2004 Nov;45(11):4119-25.PMID: 15505064 [PubMed - indexed for MEDLINE]Related articlesFree article

Fundus autofluorescence in patients with leber congenital amaurosis.

Scholl HP, Chong NH, Robson AG, Holder GE, Moore AT, Bird AC.

Invest Ophthalmol Vis Sci. 2004 Aug;45(8):2747-52.PMID: 15277500 [PubMed - indexed for MEDLINE]Related articlesFree article

Comparing rod and cone function with fundus autofluorescence images in retinitis pigmentosa.

Robson AG, Egan C, Holder GE, Bird AC, Fitzke FW.

Adv Exp Med Biol. 2003;533:41-7. No abstract available. PMID: 15180246 [PubMed - indexed for MEDLINE]Related articles

Juvenile neuronal ceroid lipofuscinosis (Batten disease) CLN3 mutation (Chrom 16p11.2) with different phenotypes in a sibling pair and low intensity in vivo autofluorescence.

Mantel I, Brantley MA Jr, Bellmann C, Robson AG, Holder GE, Taylor A, Anderson G, Moore AT.

Klin Monbl Augenheilkd. 2004 May;221(5):427-30.PMID: 15162299 [PubMed - indexed for MEDLINE]Related articles

Pattern ERG correlates of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.

Robson AG, El-Amir A, Bailey C, Egan CA, Fitzke FW, Webster AR, Bird AC, Holder GE.

Invest Ophthalmol Vis Sci. 2003 Aug;44(8):3544-50.PMID: 12882805 [PubMed - indexed for MEDLINE]Related articlesFree article

Macular pigment density and distribution: comparison of fundus autofluorescence with minimum motion photometry.

Robson AG, Moreland JD, Pauleikhoff D, Morrissey T, Holder GE, Fitzke FW, Bird AC, van Kuijk FJ.

Vision Res. 2003 Jul;43(16):1765-75.PMID: 12818346 [PubMed - indexed for MEDLINE]Related articles

Pattern ERG: clinical overview, and some observations on associated fundus autofluorescence imaging in inherited maculopathy.

Holder GE, Robson AG, Hogg CR, Kurz-Levin M, Lois N, Bird AC.

Doc Ophthalmol. 2003 Jan;106(1):17-23. Review. No abstract available. PMID: 12675481 [PubMed - indexed for MEDLINE]Related articles

Inherited retinal dystrophy and asymmetric axial length.

Francis P, Robson AG, Holder G, Moore A, Francis P, Moore A, Kaushal S.

Br J Ophthalmol. 2003 Apr;87(4):503-4. No abstract available. PMID: 12642322 [PubMed - indexed for MEDLINE]Related articlesFree article

Scalp VEPs and intra-cortical responses to chromatic and achromatic stimuli in primates.

Kulikowski JJ, Robson AG, Murray IJ.

Doc Ophthalmol. 2002 Sep;105(2):243-79.PMID: 12462446 [PubMed - indexed for MEDLINE]Related articles

Short term variability of single breath carbon monoxide transfer factor.

Robson AG, Innes JA.

Thorax. 2001 May;56(5):358-61.PMID: 11312403 [PubMed - indexed for MEDLINE]Related articlesFree article

Laboratory assessment of fitness to fly in patients with lung disease: a practical approach.

Robson AG, Hartung TK, Innes JA.

Eur Respir J. 2000 Aug;16(2):214-9.PMID: 10968494 [PubMed - indexed for MEDLINE]Related articlesFree article

Objective specification of tritanopic confusion lines using visual evoked potentials.

Robson AG, Kulikowski JJ.

Vision Res. 1998 Nov;38(21):3499-503.PMID: 9893872 [PubMed - indexed for MEDLINE]Related articles

Macular pigment and the colour-specificity of visual evoked potentials.

Moreland JD, Robson AG, Soto-Leon N, Kulikowski JJ.

Vision Res. 1998 Nov;38(21):3241-5.PMID: 9893832 [PubMed - indexed for MEDLINE]Related articles

Selective stimulation of colour mechanisms: an empirical perspective.

Kulikowski JJ, McKeefry DJ, Robson AG.

Spat Vis. 1997;10(4):379-402.PMID: 9176947 [PubMed - indexed for MEDLINE]Related articles

Specificity and selectivity of chromatic visual evoked potentials.

Kulikowski JJ, Robson AG, McKeefry DJ.

Vision Res. 1996 Nov;36(21):3397-401.PMID: 8977006 [PubMed - indexed for MEDLINE]Related articles

Topical corticosteroids potentiate mucin secretion in the normal nose.

MacGregor FB, Robson AG, Pride NB.

Clin Otolaryngol Allied Sci. 1996 Feb;21(1):76-9.PMID: 8674228 [PubMed - indexed for MEDLINE]Related articles